Taga Arens, Russo Marco, Genovese Antonio, Paglia Maria Vittoria, Manzoni Gian Camillo, Torelli Paola
Headache Centre, Department of Medicine and Surgery, University of Parma, via Gramsci 14, 43100, Parma, Italy.
Neurol Sci. 2017 May;38(Suppl 1):185-187. doi: 10.1007/s10072-017-2943-4.
The aim of the present study was to describe the characteristics of migraine with aura (MwA) in a case series of patients with headache onset before 12 years of age. We considered all consecutive patients referred to the Parma Headache Centre between 1975 and 2015 affected by MwA, diagnosed by our team of trained neurologists; the cases were subsequently reviewed applying the ICHD3-beta criteria. We then identified those cases with headache age-of-onset <12 years (i.e., "pediatric" cases), which were compared to all remaining cases. We identified 283 cases with pediatric onset (87 males and 196 females). The male-to-female ratio was 1:2.3 in both "pediatric" and "non-pediatric" cases. The time lag between MwA onset and our first evaluation was significantly higher among the pediatric cases (18.7 ± 13.3 vs 10.4 ± 10.4 years). In both groups of patients, visual aura was the most common type of aura, followed by sensory and speech disturbances; however, these two latter aura symptoms were significantly more common among pediatric cases. In this group of patients, aura without headache was significantly less frequent (1.8 vs 5.3%); furthermore, headache had migraine characteristics in a higher proportion of cases (90.1 vs 82.6%). A family history of MwA was significantly more frequent among cases with pediatric onset (31.1 vs 16.9%). Males but not females with pediatric MwA had more frequently a comorbid migraine without aura (27.6 vs 16.8%). Among cases with pediatric onset, we did not find any significant differences between males and females. In conclusion, in our very large case series of MwA, patients with headache onset before 12 years of age seem to have a specific clinical phenotype, without significant gender differences.
本研究的目的是描述一组头痛发作于12岁之前的偏头痛伴先兆(MwA)患者的特征。我们纳入了1975年至2015年间连续转诊至帕尔马头痛中心、由我们训练有素的神经科医生团队诊断为MwA的所有患者;随后根据国际头痛疾病分类第三版(ICHD3-beta)标准对这些病例进行复查。然后我们确定了头痛发病年龄<12岁的病例(即“儿科”病例),并将其与所有其余病例进行比较。我们确定了283例儿科发病病例(87例男性和196例女性)。“儿科”和“非儿科”病例的男女比例均为1:2.3。儿科病例中MwA发作与我们首次评估之间的时间间隔显著更长(18.7±13.3年 vs 10.4±10.4年)。在两组患者中,视觉先兆是最常见的先兆类型,其次是感觉和言语障碍;然而,后两种先兆症状在儿科病例中明显更常见。在这组患者中,无头痛的先兆明显较少见(1.8% vs 5.3%);此外,头痛具有偏头痛特征的病例比例更高(90.1% vs 82.6%)。儿科发病病例中MwA家族史明显更常见(31.1% vs 16.9%)。患有儿科MwA的男性而非女性更常合并无先兆偏头痛(27.6% vs 16.8%)。在儿科发病病例中,我们未发现男性和女性之间有任何显著差异。总之,在我们这个非常大的MwA病例系列中,头痛发作于12岁之前的患者似乎具有特定的临床表型,无明显性别差异。